BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 20231156)

  • 1. A variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: the GRACE Genetics Study.
    Buysschaert I; Carruthers KF; Dunbar DR; Peuteman G; Rietzschel E; Belmans A; Hedley A; De Meyer T; Budaj A; Van de Werf F; Lambrechts D; Fox KA
    Eur Heart J; 2010 May; 31(9):1132-41. PubMed ID: 20231156
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.
    Wauters E; Carruthers KF; Buysschaert I; Dunbar DR; Peuteman G; Belmans A; Budaj A; Van de Werf F; Lambrechts D; Fox KA
    Eur Heart J; 2013 Apr; 34(13):993-1001. PubMed ID: 23161703
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease.
    Virani SS; Brautbar A; Lee VV; MacArthur E; Morrison AC; Grove ML; Nambi V; Frazier L; Wilson JM; Willerson JT; Boerwinkle E; Ballantyne CM
    Circ J; 2012; 76(4):950-6. PubMed ID: 22322877
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Reduced risk of recurrent myocardial infarction in homozygous carriers of the chromosome 9p21 rs1333049 C risk allele in the contemporary percutaneous coronary intervention era: a prospective observational study.
    Hara M; Sakata Y; Nakatani D; Suna S; Usami M; Matsumoto S; Ozaki K; Nishino M; Sato H; Kitamura T; Nanto S; Hamasaki T; Tanaka T; Hori M; Komuro I;
    BMJ Open; 2014; 4(8):e005438. PubMed ID: 25232560
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetics of ACS and recurrent MI/cardiac death: are we getting to the heart of the (atherosclerotic) matter?
    Monraats PS; Jukema JW
    Eur Heart J; 2010 May; 31(9):1038-40. PubMed ID: 20233791
    [No Abstract]   [Full Text] [Related]  

  • 6. Polymorphisms on chromosome 9p21 confer a risk for acute coronary syndrome in a Chinese Han population.
    Zeng Q; Yuan Y; Wang S; Sun J; Zhang T; Qi M
    Can J Cardiol; 2013 Aug; 29(8):940-4. PubMed ID: 23454037
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome 9p21 polymorphism is associated with myocardial infarction but not with clinical outcome in Han Chinese.
    Peng WH; Lu L; Zhang Q; Zhang RY; Wang LJ; Yan XX; Chen QJ; Shen WF
    Clin Chem Lab Med; 2009; 47(8):917-22. PubMed ID: 19548844
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 9p21.3 Coronary Artery Disease Locus Identifies Patients With Treatment Benefit From Bariatric Surgery in the Nonrandomized Prospective Controlled Swedish Obese Subjects Study.
    Jacobson P; Peltonen M; Svensson PA; Taube M; Andersson-Assarsson JC; Sjoholm K; Bouchard C; Carlsson B; Carlsson LMS
    Circ Genom Precis Med; 2020 Oct; 13(5):460-465. PubMed ID: 32931306
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction.
    Szpakowicz A; Pepinski W; Waszkiewicz E; Maciorkowska D; Skawronska M; Niemcunowicz-Janica A; Milewski R; Dobrzycki S; Musial WJ; Kaminski KA
    PLoS One; 2013; 8(9):e72333. PubMed ID: 24069144
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.
    Horne BD; Carlquist JF; Muhlestein JB; Bair TL; Anderson JL
    Circ Cardiovasc Genet; 2008 Dec; 1(2):85-92. PubMed ID: 19956784
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Underestimated and under-recognized: the late consequences of acute coronary syndrome (GRACE UK-Belgian Study).
    Fox KA; Carruthers KF; Dunbar DR; Graham C; Manning JR; De Raedt H; Buysschaert I; Lambrechts D; Van de Werf F
    Eur Heart J; 2010 Nov; 31(22):2755-64. PubMed ID: 20805110
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction.
    Szpakowicz A; Kiliszek M; Pepinski W; Waszkiewicz E; Franaszczyk M; Skawronska M; Ploski R; Niemcunowicz-Janica A; Dobrzycki S; Opolski G; Musial WJ; Kaminski KA
    PLoS One; 2014; 9(8):e104635. PubMed ID: 25105296
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Utility of a genetic risk score to predict recurrent cardiovascular events 1 year after an acute coronary syndrome: A pooled analysis of the RISCA, PRAXY, and TRIUMPH cohorts.
    Labos C; Martinez SC; Leo Wang RH; Lenzini PA; Pilote L; Bogaty P; Brophy JM; Engert JC; Cresci S; Thanassoulis G
    Atherosclerosis; 2015 Sep; 242(1):261-7. PubMed ID: 26232166
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impact of 9p21.3 region and atherosclerosis-related genes' variants on long-term recurrent hard cardiac events after a myocardial infarction.
    Osmak GJ; Titov BV; Matveeva NA; Bashinskaya VV; Shakhnovich RM; Sukhinina TS; Kukava NG; Ruda MY; Favorova OO
    Gene; 2018 Mar; 647():283-288. PubMed ID: 29331485
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.
    Scheffold T; Kullmann S; Huge A; Binner P; Ochs HR; Schöls W; Thale J; Motz W; Hegge FJ; Stellbrink C; Dorsel T; Gülker H; Heuer H; Dinh W; Stoll M; Haltern G;
    BMC Cardiovasc Disord; 2011 Mar; 11():9. PubMed ID: 21385355
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Anaemia to predict outcome in patients with acute coronary syndromes.
    Ennezat PV; Maréchaux S; Pinçon C; Finzi J; Barrailler S; Bouabdallaoui N; Van Belle E; Montalescot G; Collet JP
    Arch Cardiovasc Dis; 2013; 106(6-7):357-65. PubMed ID: 23806304
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population.
    Gori F; Specchia C; Pietri S; Crociati L; Barlera S; Franciosi M; Nicolucci A; Signorini S; Brambilla P; Franzosi MG; ;
    BMC Med Genet; 2010 Apr; 11():60. PubMed ID: 20403154
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical application of chromosome 9p21.3 genotyping in patients with coronary artery disease.
    Nikulina S; Artyukhov I; Shesternya P; Gavrilyuk O; Maksimov V; Voyevoda M; Brusentsov D
    Exp Ther Med; 2019 Oct; 18(4):3100-3108. PubMed ID: 31572550
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A common variant on chromosome 9p21 affects the risk of myocardial infarction.
    Helgadottir A; Thorleifsson G; Manolescu A; Gretarsdottir S; Blondal T; Jonasdottir A; Jonasdottir A; Sigurdsson A; Baker A; Palsson A; Masson G; Gudbjartsson DF; Magnusson KP; Andersen K; Levey AI; Backman VM; Matthiasdottir S; Jonsdottir T; Palsson S; Einarsdottir H; Gunnarsdottir S; Gylfason A; Vaccarino V; Hooper WC; Reilly MP; Granger CB; Austin H; Rader DJ; Shah SH; Quyyumi AA; Gulcher JR; Thorgeirsson G; Thorsteinsdottir U; Kong A; Stefansson K
    Science; 2007 Jun; 316(5830):1491-3. PubMed ID: 17478679
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of the genetic markers for myocardial infarction with sudden cardiac death.
    Ivanova AA; Maksimov VN; Orlov PS; Ivanoshchuk DE; Savchenko SV; Voevoda MI
    Indian Heart J; 2017 Apr; 69 Suppl 1(Suppl 1):S8-S11. PubMed ID: 28400043
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.